A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252616



Internal ID22057226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75085910..75085910hg38UCSC Ensembl
chr2:75313037..75313037hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851968
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252616
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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